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Generation of mice harboring a Sox5 conditional null allele
Author(s) -
Dy Peter,
Han Yu,
Lefebvre Véronique
Publication year - 2008
Publication title -
genesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.093
H-Index - 110
eISSN - 1526-968X
pISSN - 1526-954X
DOI - 10.1002/dvg.20392
Subject(s) - testis determining factor , cre recombinase , biology , null allele , genetics , transcription factor , gene , allele , microbiology and biotechnology , transgene , genetically modified mouse , y chromosome
Sox5 belongs to the Sry‐related HMG box gene family, which encodes transcription factors controlling cell fate and differentiation in many lineages. Sox5 produces a long L‐Sox5 protein in neuronal, glial, neural crest, cartilage, and other cells, and a short Sox5 protein in spermatids. Sox5 −/− mice have revealed essential roles for L‐Sox5 in development but their neonatal death has prevented postnatal studies. We show here that we have generated mice harboring a conditional null allele for L‐Sox5 ( Sox5 fl+ ) by flanking the fifth coding exon with loxP sites. Cre recombinase‐mediated conversion of Sox5 fl+ into Sox5 fl− abolishes L‐Sox5 expression. Expectedly, Sox5 fl+/fl+ mice are indistinguishable from wildtype mice, and Sox5 fl−/fl− mice from Sox5 −/− mice. Moreover, the chondrodysplasia of Sox5 fl+/fl+ Sox6 fl+/fl+ Prx1Cre mice demonstrates that the two redundant chondrogenic Sox genes can be efficiently inactivated in a cell type‐specific manner. This Sox5 conditional null allele will be valuable in further uncovering the in vivo roles of L‐Sox5. genesis 46:294–299, 2008. © 2008 Wiley‐Liss, Inc.